Quality Control Specialist

3 semanas atrás

Loures, Lisboa, Portugal Hovione Tempo inteiro

About Hovione

Hovione is an independent family-owned international group of companies dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market.

We are a Market Leader with over 1950 team members from 36 different nationalities, located across Asia, Europe and North America.

Our people are the main asset for our continued success. We reach for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients.

Job Description:

As a Quality Control Specialist, you will be responsible for defining and implementing quality control techniques to verify the quality of raw materials, intermediate and end products.

You will manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.

You will follow daily priorities to accurately and promptly perform sample analysis, meeting laboratory plan and area KPIs.

You will adhere to the laboratory testing schedule to achieve an efficient Quality Control (QC) system.

You will take responsibility for all data generated and ensure it meets applicable GMP requirements and HSE regulations.

You will maintain checklists, laboratory records and notebooks to an acceptable GMP standard and in accordance with internal procedures.

You will maintain good hygiene and housekeeping within the laboratory.

You will perform routine calibration and maintenance of designated laboratory instruments, requesting any required parts and consumables.

You will comply with high standards in QC Laboratories.

You will report discrepancies, deviations or non-conformance to QC management in accordance with internal procedures.

You will issue events and support investigation of OOS/OOT/atypical results, deviations and QC incidents.

You will communicate effectively with other internal departments using appropriate Hovione processes and IT platforms.

You will undertake additional tasks to support laboratory activities as required.

Requirements:

  • High School diploma (mandatory)
  • Qualification in relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (strong preference)
  • Relevant work experience
  • Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (preferable)
  • Experience of GMP practices and HSE standards (preferable)
  • Technical understanding of GMP practices, analytical theory and techniques
  • Clear and open communication skills (written and verbal)
  • Competent English language skills (written and verbal)
  • Ability to work in shift patterns, as required by business needs
  • Computer literate with knowledge of MS Office package

Salary Range: $60,000 - $80,000 per annum, depending on location and experience.

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